rs62508695

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs62508695(A;A)

Make rs62508695(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

12

Position

102894875

Gene

PAH

is a	snp
is	mentioned by
dbSNP	rs62508695
dbSNP (classic)	rs62508695
ClinGen	rs62508695
ebi	rs62508695
HLI	rs62508695
Exac	rs62508695
Gnomad	rs62508695
Varsome	rs62508695
LitVar	rs62508695
Map	rs62508695
PheGenI	rs62508695
Biobank	rs62508695
1000 genomes	rs62508695
hgdp	rs62508695
ensembl	rs62508695
geneview	rs62508695
scholar	rs62508695
google	rs62508695
pharmgkb	rs62508695
gwascentral	rs62508695
openSNP	rs62508695
23andMe	rs62508695
SNPshot	rs62508695
SNPdbe	rs62508695
MSV3d	rs62508695
GWAS Ctlg	rs62508695

Max Magnitude

0

ClinVar
Risk	rs62508695(A;A)
Alt	rs62508695(A;A)
Reference	Rs62508695(G;G)
Significance	Untested
Disease	not provided not specified
Variation	info
Gene	PAH
CLNDBN	not provided not specified
Reversed	1
HGVS	NC_000012.11:g.103288653C>T
CLNSRC
CLNACC	RCV000088876.3, RCV000212762.1,